Rs7536563

From SNPedia

Jump to: navigation, search
is asnp
is mentioned by
dbSNPrs7536563
hapmaprs7536563
hgdprs7536563
ensemblrs7536563
gopubmedrs7536563
scholarrs7536563
googlers7536563
pharmgkbrs7536563
hgvbaseg2prs7536563
medrefsnprs7536563
23andMers7536563
SNP Nexus

GeneFAM69A
Chromosome1
Orientationplus
Position93121633
GenotypeEffect
rs7536563(A;A)>1.12x risk
rs7536563(A;G)1.12x risk
rs7536563(G;G)common


Genotypes Magnitude Summary
Rs7536563(A;A) >1.12x risk
Rs7536563(A;G) 1.12x risk
Rs7536563(G;G) 00 common
rs7536563 has been reported in a large study to be associated with multiple sclerosis.

The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with this allele is 1.12 (CI 1.06-1.18). [PMID 17660530]

? (A;A) (A;G) (G;G)
PharmGKBPA162356166
Name
AnnotationIn a replicated GWAS of U.K. and U.S. case/parent trios, this variant was shown to be associated with multiple sclerosis risk.
GeneFAM69A
Featue
EvidencePubMed ID:17660530
Drugs
DiseasesMultiple Sclerosis
Curation LevelCurated